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Immunofluorescence Analyser - India CDSCO Medical Device Registration

Immunofluorescence Analyser is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000317_ea89a30061b8870750dea66f7be2e336_6d41247c21e079862b0c72c365c3396e. This device is marketed under the brand name Mispa Revo. The license holder is M/S Agappe Diagnostics Ltd, and it is classified as Device Class Class A. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class A
Immunofluorescence Analyser
UID: IMP/IVD/2022/000317_ea89a30061b8870750dea66f7be2e336_6d41247c21e079862b0c72c365c3396e

Brand Name

Mispa Revo

Device Class

Class A

Approving Authority

CDSCO

Product Information

Immunofluorescence Quantitative Analyzer (Mispa Revo) is an analyzer for processing and analysis of Getein test kits including markers for cardiovascular diseases, renal diseases, inflammation, fertility, diabetes mellitus, bone metabolism, tumor and thyroid. This manual contains instructions for the use of Getein1100 and general instructions for testing specimens and quality control materials.

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